Chesterite

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Chesterite
Chesterit-chains.png
Chesterite structure
General
Category Inosilicates (multiple chains)
Formula
(repeating unit)
(Mg,Fe)
17
Si
20
O
54
(OH)
6
IMA symbol Chs [1]
Strunz classification 9.DF.05
Crystal system Orthorhombic
Crystal class Pyramidal (mm2)
(same H-M symbol)
Space group A21ma
Unit cell a = 18.61 Å, b = 45.3 Å,
c = 5.29 Å, V = 4,459.64 Å3; Z = 4
Identification
Formula mass 2,074.96 g/mol
ColorColorless, pink, brown
Cleavage (110) perfect
Mohs scale hardness2-2.5
Luster Silky - pearly
Streak white
Diaphaneity transparent
Specific gravity 3.23
Optical propertiesBiaxial negative
Refractive index α=1.617, β=1.632, γ=1.64
Birefringence δ = 0.023
Pleochroism weak, pink-brown
2V angle 70°
References [2] [3] [4] [5]

Chesterite is a rare silicate mineral that can be compared to amphiboles, micas, and jimthompsonite. [3] Its chemical formula is (Mg,Fe)
17
Si
20
O
54
(OH)
6
. Chesterite is named after Chester, Vermont, where it was first described in 1977. [6] The specific geologic setting within its origin is the Carleton talc quarry in Chester, Vermont. [4]

Chesterite has an orthorhombic crystal structure, which means it has three crystallographic axes of unequal length. All of the axes are perpendicular to each other. The stacking sequence for chesterite, which is found in micas, is very similar to orthopyroxenes and orthoamphiboles. [5] [7] Chesterite is an anisotropic mineral; therefore, it allows light to travel through it at different velocities when viewed at different angles. [4] Chesterite is usually found in thin sheets within ultramafic rocks. [4]

A polytype of chesterite could be anthophyllite, which has a similar crystal structure. [7] Chesterite is used for research on stacking formations and symmetry point groups that could be possible polymorphs or polysomes of the amphibole-anthophyllite groups. [5] Chesterite has no direct usage, but some geologists or scientists generally classify it under the amphibole-anthophyllite group.

Related Research Articles

<span class="mw-page-title-main">Hornblende</span> Complex inosilicate series of minerals

Hornblende is a complex inosilicate series of minerals. It is not a recognized mineral in its own right, but the name is used as a general or field term, to refer to a dark amphibole. Hornblende minerals are common in igneous and metamorphic rocks.

<span class="mw-page-title-main">Amphibole</span> Group of inosilicate minerals

Amphibole is a group of inosilicate minerals, forming prism or needlelike crystals, composed of double chain SiO
4
tetrahedra, linked at the vertices and generally containing ions of iron and/or magnesium in their structures. Its IMA symbol is Amp. Amphiboles can be green, black, colorless, white, yellow, blue, or brown. The International Mineralogical Association currently classifies amphiboles as a mineral supergroup, within which are two groups and several subgroups.

<span class="mw-page-title-main">Phlogopite</span> Member of the mica family of phyllosilicates

Phlogopite is a yellow, greenish, or reddish-brown member of the mica family of phyllosilicates. It is also known as magnesium mica.

<span class="mw-page-title-main">Cummingtonite</span> Silicate mineral

Cummingtonite is a metamorphic amphibole with the chemical composition (Mg,Fe2+
)
2
(Mg,Fe2+
)
5
Si
8
O
22
(OH)
2
, magnesium iron silicate hydroxide.

<span class="mw-page-title-main">Anthophyllite</span>

Anthophyllite is an orthorhombic amphibole mineral: ☐Mg2Mg5Si8O22(OH)2 (☐ is for a vacancy, a point defect in the crystal structure), magnesium iron inosilicate hydroxide. Anthophyllite is polymorphic with cummingtonite. Some forms of anthophyllite are lamellar or fibrous and are classed as asbestos. The name is derived from the Latin word anthophyllum, meaning clove, an allusion to the most common color of the mineral. The Anthophyllite crystal is characterized by its perfect cleavage along directions 126 degrees and 54 degrees.

<span class="mw-page-title-main">Barytocalcite</span>

Barytocalcite is an anhydrous barium calcium carbonate mineral with the chemical formula BaCa(CO3)2. It is trimorphous with alstonite and paralstonite, that is to say the three minerals have the same formula but different structures. Baryte and quartz pseudomorphs after barytocalcite have been observed.

<span class="mw-page-title-main">Sperrylite</span>

Sperrylite is a platinum arsenide mineral with the chemical formula PtAs2 and is an opaque metallic tin white mineral which crystallizes in the isometric system with the pyrite group structure. It forms cubic, octahedral or pyritohedral crystals in addition to massive and reniform habits. It has a Mohs hardness of 6 - 7 and a very high specific gravity of 10.6.

Alloclasite is a sulfosalt mineral. It is a member of the arsenopyrite group. Alloclasite crystallizes in the monoclinic system and typically forms as columnar to radiating acicular prismatic clusters. It is an opaque steel-gray to silver-white, with a metallic luster and a black streak. It is brittle with perfect cleavage, a Mohs hardness of 5 and a specific gravity of 5.91–5.95.

<span class="mw-page-title-main">Tschermakite</span> Amphibole, double chain inosilicate mineral

The endmember hornblende tschermakite (☐Ca2(Mg3Al2)(Si6Al2)O22(OH)2) is a calcium rich monoclinic amphibole mineral. It is frequently synthesized along with its ternary solid solution series members tremolite and cummingtonite so that the thermodynamic properties of its assemblage can be applied to solving other solid solution series from a variety of amphibole minerals.

<span class="mw-page-title-main">Gedrite</span>

Gedrite is a crystal belonging to the orthorhombic ferromagnesian subgroup of the amphibole supergroup of the double chain inosilicate minerals with the ideal chemical formula Mg2(Mg3Al2)(Si6Al2)O22(OH)2.

<span class="mw-page-title-main">Dollaseite-(Ce)</span> Epidote supergroup, sorosilicate mineral

Dollaseite-(Ce) is a sorosilicate end-member epidote rare-earth mineral which was discovered by Per Geijer (1927) in the Ostanmossa mine, Norberg district, Sweden. Dollaseite-(Ce), although not very well known, is part of a broad epidote group of minerals which are primarily silicates, the most abundant type of minerals on earth. Dollaseite-(Ce) forms as dark-brown subhedral crystals primarily in Swedish mines. With the ideal chemical formula, CaREE3+
Mg
2
AlSi
3
O
11
,(OH)F
, dollaseite-(Ce) can be partially identified by its content of the rare earth element cerium.

Bityite is considered a rare mineral, and it is an endmember to the margarite mica sub-group found within the phyllosilicate group. The mineral was first described by Antoine François Alfred Lacroix in 1908, and later its chemical composition was concluded by Professor Hugo Strunz. Bityite has a close association with beryl, and it generally crystallizes in pseudomorphs after it, or in cavities associated with reformed beryl crystals. The mineral is considered a late-stage constituent in lithium bearing pegmatites, and has only been encountered in a few localities throughout the world. The mineral was named by Lacroix after Mt. Bity, Madagascar from where it was first discovered.

Bystrite is a silicate mineral with the formula (Na,K)7Ca(Si6Al6)O24S4.5•(H2O), and a member of the cancrinite mineral group. It is a hexagonal crystal, with a 3m point group. The mineral may have been named after the Malaya Bystraya deposits in Russia, where it was found.

Grandreefite is a rare secondary lead sulfate-fluoride mineral with a general chemical formula, Pb2SO4F2. It is named for the location in which it was discovered in 1989, the Grand Reef Mine in Graham County, Arizona.

<span class="mw-page-title-main">Karlite</span>

Karlite (kar'-lite) is a silky white to light green orthorhombic borate mineral, not to be confused with tremolite-actinolite. It has a general formula of Mg7(BO3)3(OH)4Cl. Karlite is named in honor of Franz Karl (1918–1972), professor of mineralogy and petrography at Christian Albrechts University in Kiel, Germany, for his studies of the geology of the eastern Alps.

<span class="mw-page-title-main">Kanoite</span>

Kanoite is a light pinkish brown silicate mineral that is found in metamorphic rocks. It is an inosilicate and has a chemical formula of (Mg,Mn2+)2Si2O6. It is a member of pyroxene group and clinopyroxene subgroup.

<span class="mw-page-title-main">Vlasovite</span>

Vlasovite is a rare inosilicate (chain silicate) mineral with sodium and zirconium, with the chemical formula Na2ZrSi4O11. It was discovered in 1961 at Vavnbed Mountain in the Lovozero Massif, in the Northern Region of Russia. The researchers who first identified it, R P Tikhonenkova and M E Kazakova, named it for Kuzma Aleksevich Vlasov (1905–1964), a Russian mineralogist and geochemist who studied the Lovozero massif, and who was the founder of the Institute of Mineralogy, Geochemistry, and Crystal Chemistry of Rare Elements, Moscow, Russia.

<span class="mw-page-title-main">Tuperssuatsiaite</span>

Tuperssuatsiaite is a rare clay mineral found in Greenland, Namibia and Brazil. It is a hydrated phyllosilicate of sodium and iron.

<span class="mw-page-title-main">Jimthompsonite</span>

Jimthompsonite is a magnesium iron silicate mineral with chemical formula (Mg,Fe2+)5Si6O16(OH)2. It is a triple chain silicate (or inosilicate) along with clinojimthompsonite and chesterite. They were described in 1977 by Burham and Veblen. They attracted great mineralogical attention because they were the first examples of new chain silicate structures among a large group known as biopyriboles whose name is derived from the words biotite, pyroxene, and amphiboles.

<span class="mw-page-title-main">Ephesite</span>

Ephesite is a rare member of the mica silicate mineral group, phyllosilicate. It is restricted to quartz-free, alumina rich mineral assemblages and has been found in South African deposits in the Postmasburg district as well as Ephesus, Turkey.

References

  1. Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine. 85 (3): 291–320. Bibcode:2021MinM...85..291W. doi: 10.1180/mgm.2021.43 . S2CID   235729616.
  2. Mineralienatlas
  3. 1 2 Ralph, Joylon and Ida, Chau. "Chesterite." http://www.mindat.org/min-997.html.
  4. 1 2 3 4 "Chesterite Mineral Data." http://webmineral.com/data/Chesterite.shtml. Accessed 3 November 2010.
  5. 1 2 3 Veblen, D.R. and Burnham, C.W. (1978) New biopyriboles from Chester, Vermont: II. The crystal chemistry of jimthompsonite, clinojimthompsonite, and Chesterite, and the amphibole-mica reaction. American Mineralogist, 63, 1053-1073.
  6. Konishi, Hiromi, Reijo, Alviola, and Buseck, Peter R. (2004) 2111 biopyribole intermediate between pyroxene and amphibole: Artifact or natural product? American Mineralogist, 89, 15-19.
  7. 1 2 Wyckoff, R.W.G. (1968) Crystal Structures (Second edition). 310-314 p. University of Arizona, Tucson, Arizona.